FDA Inspection 1258117 — Enrique Lara Gonzalez, MD

Enrique Lara Gonzalez, MD — FEI 3032209898

The FDA completed an inspection of Enrique Lara Gonzalez, MD on Dec 6, 2024 in Merida. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 6, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Merida (Mexico)

Additional Details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.